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FDA 510(k)

ACRYDERM ADVANCED WOUND DRESSING

K-Number: K943781 · 1994-10-04

ApplicantAcrymed, Inc.
Decision Date1994-10-04
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ACRYDERM ADVANCED WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Acrymed, Inc.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K943781. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ACRYDERM ADVANCED WOUND DRESSING?

ACRYDERM ADVANCED WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Acrymed, Inc.. The 510(k) number is K943781.

When did ACRYDERM ADVANCED WOUND DRESSING receive FDA 510(k) clearance?

ACRYDERM ADVANCED WOUND DRESSING received FDA 510(k) clearance on 1994-10-04, under 510(k) number K943781.

Who is the listed applicant for ACRYDERM ADVANCED WOUND DRESSING?

The FDA 510(k) record lists Acrymed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACRYDERM ADVANCED WOUND DRESSING?

The FDA product code for ACRYDERM ADVANCED WOUND DRESSING is KMF.

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Other records listing Acrymed, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K091354ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSINGK083103ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #BK082459ACRYDERM ABSORBENT OXYGEN DRESSINGK070333ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GELK061232ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006K011994ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

View all 14 devices →

Related Devices (Code: KMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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